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Comparison of the efficacy of three active warming methods during perioperative lumbar surgery of aged patients: a randomized controlled trial

Comparison of the efficacy of three active warming methods during perioperative lumbar surgery of aged patients: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031845
Enrollment
Unknown
Registered
2020-04-12
Start date
2019-12-01
Completion date
Unknown
Last updated
2020-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Group 1:Forced-air warming blanket
Group 2:Resistive-polymer blanket
Group 3:Intravenous fluid warming

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-II grade; 2. Aged >= 65 years; 3. BMI20-30kg/m2; 4. Voluntary participation in the trial and signing informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant women; 2. A history of craniocerebral disease; 3. Preoperative body temperature was greater than 37.5 degrees C; 4. Recent infection; 5. Inadequate thermoregulation; 6. Difficulty in temperature measurement; 7. Heart disease (pacemaker placement, frequent arrhythmia, atrial fibrillation, etc.); 8. Pulmonary diseases (pulmonary infection, emphysema, chronic obstructive pulmonary disease, etc.); 9. Drug allergy; 10. Known difficult airways; 11. Preoperative hemoglobin concentration and Hct were not in the normal range; 12. Renal impairment (upper limit of normal values of BUN and/or Cr>); 13. Liver function damage (ALT and/or AST>1.5 times normal reference range); 14. Suffering from mental or neurological diseases or inability to express one's will properly; 15. Long-term use of sedatives, analgesics and psychotropic drugs; 16. Coagulation dysfunction (PT/APTT above the upper limit of reference); 17. Arm disability, blood pressure and oxygen saturation monitoring can only be located on the same arm; 18. History of hypertension and systolic blood pressure > 180 or diastolic blood pressure > 110 mmHg did not decrease for two consecutive measurements; 19. Neuromuscular diseases (specifically paraplegia, myasthenia gravis).

Design outcomes

Primary

MeasureTime frame
esophageal temperature;body surface temperature;

Countries

China

Contacts

Public ContactHan Lin

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

nanlinhannansh@qq.com+86 1586871083

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026